Canonical Allele Identifier: CA2650500794
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675699_215675702del , CM000663.2:g.215675699_215675702del GRCh38
NC_000001.10:g.215849041_215849044del , CM000663.1:g.215849041_215849044del GRCh37
NC_000001.9:g.213915664_213915667del NCBI36
NG_009497.1:g.752696_752699del
NG_009497.2:g.752748_752751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-85_12295-82del MANE Select ENSP00000305941.3:n.12295-85_12295-82del
ENST00000674083.1:c.12295-85_12295-82del ENSP00000501296.1:n.12295-85_12295-82del
ENST00000307340.7:c.12295-85_12295-82del ENSP00000305941.3:n.12295-85_12295-82del
NM_206933.2:c.12295-85_12295-82del NP_996816.2:n.12295-85_12295-82del
NM_206933.3:c.12295-85_12295-82del NP_996816.2:n.12295-85_12295-82del
NM_206933.4:c.12295-85_12295-82del MANE Select NP_996816.3:n.12295-85_12295-82del